| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:32971883-32972284 | Common:4; Rare:119 | ||||
| chr19:33081126-33081233 | Common:1; Rare:46 | ||||
| chr19:33373548-33373821 | Common:2; Rare:90 | ||||
| chr19:33521756-33521956 | Common:1; Rare:63; Clinvar:5 | ||||
| chr19:34172351-34172597 | Rare:102 | ||||
| chr19:34254484-34254603 | Rare:37 | ||||
| chr19:34365086-34365333 | Common:1; Rare:107; Clinvar (pathogenic):1 | ||||
| chr19:34428310-34428425 | Rare:49 | ||||
| chr19:34677487-34677758 | Common:7; Rare:79 | ||||
| chr19:34733989-34734272 | Common:2; Rare:82 | ||||
| chr19:34926826-34926913 | Common:1; Rare:36 | ||||
| chr19:35000202-35000470 | Common:4; Rare:68 | ||||
| chr19:35155054-35155277 | Rare:48 | ||||
| chr19:35545454-35545734 | Common:4; Rare:94 | ||||
| chr19:35628880-35629124 | Common:4; Rare:76 |